@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP524771.RAyGSytMtuzBVv23IY60lq1xaTuCQRTfnUNbAh7leJqas
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP524771.RAyGSytMtuzBVv23IY60lq1xaTuCQRTfnUNbAh7leJqas130_head
{
this:
np:hasAssertion
dgn-np:NP524771.RAyGSytMtuzBVv23IY60lq1xaTuCQRTfnUNbAh7leJqas130_assertion
;
np:hasProvenance
dgn-np:NP524771.RAyGSytMtuzBVv23IY60lq1xaTuCQRTfnUNbAh7leJqas130_provenance
;
np:hasPublicationInfo
dgn-np:NP524771.RAyGSytMtuzBVv23IY60lq1xaTuCQRTfnUNbAh7leJqas130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP524771.RAyGSytMtuzBVv23IY60lq1xaTuCQRTfnUNbAh7leJqas130_assertion
a
np:Assertion
.
dgn-np:NP524771.RAyGSytMtuzBVv23IY60lq1xaTuCQRTfnUNbAh7leJqas130_provenance
a
np:Provenance
.
dgn-np:NP524771.RAyGSytMtuzBVv23IY60lq1xaTuCQRTfnUNbAh7leJqas130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP524771.RAyGSytMtuzBVv23IY60lq1xaTuCQRTfnUNbAh7leJqas130_assertion
{
miriam-gene:1630
a
ncit:C16612
.
lld:C0027819
a
ncit:C7057
.
dgn-gda:DGNc96c5c10a9092cd2965a147d52fedfb3
sio:SIO_000628
miriam-gene:1630
,
lld:C0027819
;
a
sio:SIO_001121
.
}
dgn-np:NP524771.RAyGSytMtuzBVv23IY60lq1xaTuCQRTfnUNbAh7leJqas130_provenance
{
dgn-np:NP524771.RAyGSytMtuzBVv23IY60lq1xaTuCQRTfnUNbAh7leJqas130_assertion
dcterms:description
"[Our results suggested that mutations of the DCC gene may be involved in the pathogenesis of neuroblastomas but failed to account for the relatively high frequency of the altered expression, implying that other mechanisms are responsible for the inactivation of the DCC gene in neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:9288786
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP524771.RAyGSytMtuzBVv23IY60lq1xaTuCQRTfnUNbAh7leJqas130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:15+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}